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1.
J Biosci ; 2005 Sep; 30(4): 469-74
Article in English | IMSEAR | ID: sea-110664

ABSTRACT

Nine major transfer RNA (tRNA) gene clusters were analysed in various Vibrio cholerae strains. Of these, only the tRNA operon I was found to differ significantly in V. cholerae classical (sixth pandemic) and El Tor (seventh pandemic) strains. Amongst the sixteen tRNA genes contained in this operon, genes for tRNA Gln3 (CAA) and tRNA Leu6 (CUA) were absent in classical strains as compared to El Tor strains. The observation strongly supported the view that the above two pandemic strains constitute two different clones.


Subject(s)
Operon/genetics , RNA, Transfer/chemistry , Vibrio cholerae/classification , rRNA Operon/genetics
2.
Braz. j. microbiol ; 36(2): 177-183, Apr.-June 2005. ilus
Article in English | LILACS | ID: lil-421722

ABSTRACT

Operons ribossomais têm sido instrumentos importantes na caracterizacão de comunidades microbianas e no estudo de relacionamentos entre microrganismos, principalmente em bactérias do ácido láctico. Operons ribossomais da linhagem probiótica, Lactobacillus delbrueckii UFV H2b20, foram parcialmente caracterizados. Um banco genômico da linhagem foi construído e os clones, contendo parte do operon ribossomal, foram subclonados pelo método de "shot gun", para em seguida serem seqüenciados com primer "forward". As seqüências indicaram a presenca da extremidade 3' do rDNA 16S seguida da região espacadora curta 1 (16S-23S) e a presenca da extremidade 3' do rDNA 23S seguido da região espacadora 2 (23S-5S), que por sua vez precedia o rDNA 5S. Adjacente ao gene rDNA 5S deste operon rrn uma região codificadora de 6 tRNAs foi detectada.


Subject(s)
DNA, Ribosomal , Genomic Library , In Vitro Techniques , Lactic Acid , Lactobacillus , RNA, Ribosomal , rRNA Operon , Methods , Sampling Studies
3.
Genet. mol. res. (Online) ; 3(1): 64-75, Mar. 2004.
Article in English | LILACS | ID: lil-417584

ABSTRACT

The repertoire of 4,431 open reading frames (ORFs), eight rRNA operons and 98 tRNA genes of Chromobacterium violaceum must be expressed in a regulated manner for successful adaptation to a wide variety of environmental conditions. To accomplish this feat, the organism relies on protein machineries involved in transcription, RNA processing and translation. Analysis of the C. violaceum genome showed that transcription initiation, elongation and termination are performed by the five well-known RNA polymerase subunits, five categories of sigma 70 factors, one sigma 54 factor, as well as six auxiliary elongation and termination factors. RNA processing is performed by a variety of endonucleases and exonucleases, such as ribonuclease H, ribonuclease E, ribonuclease P, and ribonuclease III, in addition to poly(A) polymerase and specific methyltransferases and pseudouridine synthases. ORFs for all ribosomal proteins, except S22, were found. Only 19 aminoacyl-tRNA synthetases were found, in addition to three aminoacyl-tRNA synthetase-related proteins. Asparaginyl-tRNA (Asn) is probably obtained by enzymatic modification of a mischarged aminoacyl-tRNA. The translation factors IF-1, IF-2, IF-3, EF-Ts, EF-Tu, EF-G, RF-1, RF-2 and RF-3 are all present in the C. violaceum genome, although the absence of selB suggests that C. violaceum does not synthesize selenoproteins. The components of trans-translation, tmRNA and associated proteins, are present in the C. violaceum genome. Finally, a large number of ORFs related to regulation of gene expression were also found, which was expected, considering the apparent adaptability of this bacterium


Subject(s)
Adaptation, Physiological/genetics , Chromobacterium/genetics , Gene Expression Regulation, Bacterial/genetics , Chromobacterium/physiology , Open Reading Frames/genetics , Genome, Bacterial , RNA, Transfer/genetics , rRNA Operon , Gene Expression Regulation, Bacterial/physiology , Transcription, Genetic
4.
P. R. health sci. j ; 16(3): 251-4, sept. 1997. ilus
Article in English | LILACS | ID: lil-212527

ABSTRACT

Several reports indicate geographic variation of isolates of Pneumocystis carinii hominis. We have sequenced the internal transcribed spacer (ITS) region and large subunit Group I intron of rRNA genes from P. carinii DNA obtained from two patients from Puerto Rico. Both can be subclassified as Type II, according to the sequence of the ITS region. A system capable of identifying individual isolates will be an essential tool for epidemiological studies of the organism. The amplification of DNA from fixed tissues may facilitate the processing of a large number of samples.


Subject(s)
Humans , Pneumocystis carinii/genetics , rRNA Operon/genetics , Base Sequence , Molecular Sequence Data , Puerto Rico
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